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. 1991 Feb;173(4):1536–1543. doi: 10.1128/jb.173.4.1536-1543.1991

Expression of gene 1.2 and gene 10 of bacteriophage T7 is lethal to F plasmid-containing Escherichia coli.

C K Schmitt 1, I J Molineux 1
PMCID: PMC207293  PMID: 1995595

Abstract

Plasmids expressing bacteriophage T7 gene 1.2 or gene 10 DNA transform F plasmid-containing strains of Escherichia coli only at low efficiency, though they transform plasmid-free strains normally. The gene products T7 gp1.2 and T7 gp10 appear to be the toxic agents, and their effects are directed towards the product of the F pifA gene, PifA. T7 gp1.2 and gp10 are also the two targets of the pif exclusion system of F, and their synthesis normally triggers the abortive infection of T7 in pifA+ hosts. The properties of plasmids containing T7 gene 1.2 or 10 suggest that they can be used to study the molecular mechanisms of phage exclusion in model systems that avoid the pleiotropic dysfunctions associated with an abortive infection.

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Selected References

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  1. Bailone A., Sommer S., Devoret R. Mini-F plasmid-induced SOS signal in Escherichia coli is RecBC dependent. Proc Natl Acad Sci U S A. 1985 Sep;82(17):5973–5977. doi: 10.1073/pnas.82.17.5973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beck P. J., Condreay J. P., Molineux I. J. Expression of the unassembled capsid protein during infection of Shigella sonnei by bacteriophage T7 results in DNA damage that is repairable by bacteriophage T3, but not T7, DNA ligase. J Bacteriol. 1986 Jul;167(1):251–256. doi: 10.1128/jb.167.1.251-256.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Beck P. J., Molineux I. J. Defective transcription of the right end of bacteriophage T7 DNA during an abortive infection of F plasmid-containing Escherichia coli. J Bacteriol. 1991 Feb;173(3):947–954. doi: 10.1128/jb.173.3.947-954.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Blumberg D. D., Malamy M. H. Evidence for the presence of nontranslated T7 late mRNA in infected F'(PIF+) episome-containing cells. J Virol. 1974 Feb;13(2):378–385. doi: 10.1128/jvi.13.2.378-385.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Britton J. R., Haselkorn R. Permeability lesions in male Escherichia coli infected with bacteriophage T7. Proc Natl Acad Sci U S A. 1975 Jun;72(6):2222–2226. doi: 10.1073/pnas.72.6.2222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Champness W. C., Snyder L. Bacteriophage T4 gol site: sequence analysis and effects of the site on plasmid transformation. J Virol. 1984 May;50(2):555–562. doi: 10.1128/jvi.50.2.555-562.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Champness W. C., Snyder L. The gol site: a cis-acting bacteriophage T4 regulatory region that can affect expression of all the T4 late genes. J Mol Biol. 1982 Mar 15;155(4):395–407. doi: 10.1016/0022-2836(82)90478-8. [DOI] [PubMed] [Google Scholar]
  8. Cohen S. N., Chang A. C., Hsu L. Nonchromosomal antibiotic resistance in bacteria: genetic transformation of Escherichia coli by R-factor DNA. Proc Natl Acad Sci U S A. 1972 Aug;69(8):2110–2114. doi: 10.1073/pnas.69.8.2110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Condit R. C. F factor-mediated inhibition of bacteriophage T7 growth: increased membrane permeability and decreased ATP levels following T7 infection of male Escherichia coli. J Mol Biol. 1975 Oct 15;98(1):45–59. doi: 10.1016/s0022-2836(75)80100-8. [DOI] [PubMed] [Google Scholar]
  10. Condreay J. P., Molineux I. J. Synthesis of the capsid protein inhibits development of bacteriophage T3 mutants that abortively infect F plasmid-containing cells. J Mol Biol. 1989 Jun 5;207(3):543–554. doi: 10.1016/0022-2836(89)90463-4. [DOI] [PubMed] [Google Scholar]
  11. Condreay J. P., Wright S. E., Molineux I. J. Nucleotide sequence and complementation studies of the gene 10 region of bacteriophage T3. J Mol Biol. 1989 Jun 5;207(3):555–561. doi: 10.1016/0022-2836(89)90464-6. [DOI] [PubMed] [Google Scholar]
  12. Cram D., Ray A., Skurray R. Molecular analysis of F plasmid pif region specifying abortive infection of T7 phage. Mol Gen Genet. 1984;197(1):137–142. doi: 10.1007/BF00327934. [DOI] [PubMed] [Google Scholar]
  13. Cram H. K., Cram D., Skurray R. F plasmid pif region: Tn1725 mutagenesis and polypeptide analysis. Gene. 1984 Dec;32(1-2):251–254. doi: 10.1016/0378-1119(84)90053-2. [DOI] [PubMed] [Google Scholar]
  14. Duckworth D. H., Glenn J., McCorquodale D. J. Inhibition of bacteriophage replication by extrachromosomal genetic elements. Microbiol Rev. 1981 Mar;45(1):52–71. doi: 10.1128/mr.45.1.52-71.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Dunn J. J., Studier F. W. Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elements. J Mol Biol. 1983 Jun 5;166(4):477–535. doi: 10.1016/s0022-2836(83)80282-4. [DOI] [PubMed] [Google Scholar]
  16. Jackson R., Cram D., Ray A., DiBerardino D., Skurray R. Cloning and analysis of pif, replication and leading regions of the F plasmid. Mol Gen Genet. 1984;197(1):129–136. doi: 10.1007/BF00327933. [DOI] [PubMed] [Google Scholar]
  17. Jaffé A., Ogura T., Hiraga S. Effects of the ccd function of the F plasmid on bacterial growth. J Bacteriol. 1985 Sep;163(3):841–849. doi: 10.1128/jb.163.3.841-849.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kao C., Snyder L. The lit gene product which blocks bacteriophage T4 late gene expression is a membrane protein encoded by a cryptic DNA element, e14. J Bacteriol. 1988 May;170(5):2056–2062. doi: 10.1128/jb.170.5.2056-2062.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kennedy M., Chandler M., Lane D. Mapping and regulation of the pifC promoter of the F plasmid. Biochim Biophys Acta. 1988 May 6;950(1):75–80. doi: 10.1016/0167-4781(88)90075-9. [DOI] [PubMed] [Google Scholar]
  20. Low K. B. Escherichia coli K-12 F-prime factors, old and new. Bacteriol Rev. 1972 Dec;36(4):587–607. doi: 10.1128/br.36.4.587-607.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Miller J. F., Lanka E., Malamy M. H. F factor inhibition of conjugal transfer of broad-host-range plasmid RP4: requirement for the protein product of pif operon regulatory gene pifC. J Bacteriol. 1985 Sep;163(3):1067–1073. doi: 10.1128/jb.163.3.1067-1073.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Miller J. F., Malamy M. H. Identification of the pifC gene and its role in negative control of F factor pif gene expression. J Bacteriol. 1983 Oct;156(1):338–347. doi: 10.1128/jb.156.1.338-347.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Miller J. F., Malamy M. H. Regulation of the F-factor pif operon: pifO, a site required in cis for autoregulation, titrates the pifC product in trans. J Bacteriol. 1984 Oct;160(1):192–198. doi: 10.1128/jb.160.1.192-198.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Molineux I. J., Mooney P. Q., Spence J. L. Recombinants between bacteriophages T7 and T3 which productively infect F-plasmid-containing strains of Escherichia coli. J Virol. 1983 Jun;46(3):881–894. doi: 10.1128/jvi.46.3.881-894.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Molineux I. J., Schmitt C. K., Condreay J. P. Mutants of bacteriophage T7 that escape F restriction. J Mol Biol. 1989 Jun 5;207(3):563–574. doi: 10.1016/0022-2836(89)90465-8. [DOI] [PubMed] [Google Scholar]
  26. Morrison T. G., Blumberg D. D., Malamy M. H. T7 protein synthesis in F' episome-containing cells: assignment of specific proteins to three translational groups. J Virol. 1974 Feb;13(2):386–393. doi: 10.1128/jvi.13.2.386-393.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Morrison T. G., Malamy M. H. T7 translational control mechanisms and their inhibiton by F factors. Nat New Biol. 1971 May 12;231(19):37–41. doi: 10.1038/newbio231037a0. [DOI] [PubMed] [Google Scholar]
  28. Novick R. P. Plasmid incompatibility. Microbiol Rev. 1987 Dec;51(4):381–395. doi: 10.1128/mr.51.4.381-395.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Rotman G. S., Cooney R., Malamy M. H. Cloning of the pif region of the F sex factor and identification of a pif protein product. J Bacteriol. 1983 Jul;155(1):254–264. doi: 10.1128/jb.155.1.254-264.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Saito H., Richardson C. C. Genetic analysis of gene 1.2 of bacteriophage T7: isolation of a mutant of Escherichia coli unable to support the growth of T7 gene 1.2 mutants. J Virol. 1981 Jan;37(1):343–351. doi: 10.1128/jvi.37.1.343-351.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Saito H., Richardson C. C. Processing of mRNA by ribonuclease III regulates expression of gene 1.2 of bacteriophage T7. Cell. 1981 Dec;27(3 Pt 2):533–542. doi: 10.1016/0092-8674(81)90395-0. [DOI] [PubMed] [Google Scholar]
  32. Schmitt M. P., Beck P. J., Kearney C. A., Spence J. L., DiGiovanni D., Condreay J. P., Molineux I. J. Sequence of a conditionally essential region of bacteriophage T3, including the primary origin of DNA replication. J Mol Biol. 1987 Feb 5;193(3):479–495. doi: 10.1016/0022-2836(87)90261-0. [DOI] [PubMed] [Google Scholar]
  33. Tanimoto K., Iino T. Transfer inhibition of RP4 by F factor. Mol Gen Genet. 1983;192(1-2):104–109. doi: 10.1007/BF00327654. [DOI] [PubMed] [Google Scholar]
  34. Young E. T., Menard R. C. Analysis of the template activity of bacteriophage T7 messenger RNAs during infection of male and female strains of Escherichia coli. J Mol Biol. 1975 Nov 25;99(1):167–184. doi: 10.1016/s0022-2836(75)80166-5. [DOI] [PubMed] [Google Scholar]

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